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║        Biologist-Biotechnologist | Postdoc | Liquid Biopsy Specialist    ║
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About Me

I’m a postdoctoral researcher at the Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, specialising in liquid biopsy development and circulating cell-free DNA analysis. My work combines long-read and short-read sequencing technologies with computational biology to develop novel diagnostic tools for metabolic disorders and obesity-related diseases.

    ┌─────────────────────────────────────────────────────────────┐
    │  RESEARCH FOCUS                                             │
    ├─────────────────────────────────────────────────────────────┤
    │  → Liquid biopsy development                                │
    │  → Cell-free DNA biology and diagnostics                    │
    │  → Long-read and short-read sequencing                      │
    │  → Epigenetic biomarkers in metabolic disease               │
    │  → Machine learning for clinical applications               │
    └─────────────────────────────────────────────────────────────┘

Current Projects

MethylSense Logo

MethylSense: ML-Powered cfDNA Methylation Diagnostics

[In Development]

Building machine learning models that leverage cell-free DNA methylation patterns from nanopore sequencing for disease prediction and clinical decision support in metabolic disorders. Based on recent research demonstrating the diagnostic potential of cfDNA methylation profiling in obesity and related conditions.

Preprint: bioRxiv 2025.04.11.648151


NanoporeToBED Pipeline

NanoporeToBED Pipeline Logo
  [Nanopore Data] → [Processing] → [BED Format] → [Downstream Analysis]
       |                |              |                   |
    Raw FAST5      Basecalling    Methylation         Visualisation
    Raw POD5       Alignment      Modification        Statistical
                   QC Steps       Calling             Analysis

github.com/markusdrag/NanoporeToBED-Pipeline

A streamlined bioinformatics workflow for converting nanopore sequencing data into analysis-ready BED format for epigenetic studies.


GenomeToWindows

GenomeToWindows Logo
  [Ensembl/UCSC] → [Download] → [Index] → [Window] → [BED Output]
       |              |           |          |            |
   Genome DBs    Auto-detect  samtools   bedtools    Custom sizes
   100+ spp.     Latest       faidx      makewindows  (1-25kb)

github.com/markusdrag/GenomeToWindows

Automated genome downloading and windowing tool for MethylSense preprocessing. Downloads genomes from Ensembl or UCSC and generates genomic windows with flexible sizes (1kb-25kb). Features automatic fallback between databases, progress tracking, dry-run mode, and automated environment setup.

Key Features:


Tech Stack

┌──────────────────┬──────────────────────────────────────────────┐
│ Languages        │ R, Bash, Python                              │
├──────────────────┼──────────────────────────────────────────────┤
│ Workflows        │ Nextflow, Shell scripting                    │
├──────────────────┼──────────────────────────────────────────────┤
│ Nanopore Tools   │ Dorado, Modkit, Minimap2, Samtools           │
├──────────────────┼──────────────────────────────────────────────┤
│ R Packages       │ ggplot2, dplyr, tidyverse, DESeq2            │
├──────────────────┼──────────────────────────────────────────────┤
│ Stat Genetics    │ PLINK, Matrix eQTL, FastQTL                  │
├──────────────────┼──────────────────────────────────────────────┤
│ Infrastructure   │ HPC environments, Linux, Git                 │
└──────────────────┴──────────────────────────────────────────────┘

Selected Publications & Research

Google Scholar: Markus H. Drag

Selected publications:

Liquid Biopsy & cfDNA:

Systems Genomics & eQTLs:

Transcriptomics:


Let’s Connect

    ╭───────────────────────────────────────────────────────────╮
    │  LinkedIn:  linkedin.com/in/markusdrag                    │
    │  Scholar:   scholar.google.com/citations?user=KHoAwvoAAAAJ│
    │  Email:     markus.drag@sund.ku.dk                        │
    ╰───────────────────────────────────────────────────────────╯

  "From each cfDNA fragment to biological insight—one methylation mark at a time"